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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020710Generated: October 27, 2026

Methanesulfonic Acid → HCID 178465170, compound

https://huagongshe.com/reaction/1020710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium CarbonateHCID 10340—
ReactantO-benzyl-N-((tert-butoxy)carbonyl)-L-tyrosineHCID 98763—
ReactantHCID 178465172HCID 178465172—
SolventDichloromethaneHCID 6344—
ProductHCID 178465170HCID 178465170—

Reaction Steps

Boc-Tyr(Bn)-D-Leu-Leu-Arg(Ts)-Pro-NHEt was prepared from Boc-D-Leu-Leu-Arg(Ts)-Pro-NHEt obtained in Example 2 and Boc-Tyr(Bn) by the same procedure as Example 2. To a solution composed of this compound (0.46 g) and dichloromethane (5 ml), methanesulfonic acid (0.42 g) was added at room temperature, and the resulting mixture was stirred at room temperature for 1 hour, thereby the Boc group was removed (reaction conversion ratio: 99.9%). After the reaction, 5% aqueous sodium carbonate solution (5 ml) was added thereto, and the resulting mixture was stirred for 15 minutes, and then, the aqueous layer was separated off. After Boc-Ser (Bn) (0.19 g) and HOBt monohydrate (0.12 g) were added to the obtained dichloromethane solution of Tyr(Bn)-D-Leu-Leu-Arg(Ts)-Pro-NHEt, the reaction solution was cooled with ice. Then, EDC hydrochloride (0.15 g) was added thereto, and the resulting mixture was stirred for 1 hour. Subsequently, the temperature of the mixture was raised to room temperature and the mixture was stirred for 15 hours, thereby a condensation reaction was carried out (reaction conversion ratio: 99.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716439B2
Source datasetuspto-grants-2014_05
ORD IDord-70799e3c940840d780a5be6a7a4657c9
Source noteuspto-grants-2014_05