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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755474Generated: November 2, 2026

Sodium borohydride → (S)-N-((S)-1-((S)-1-((S)-1-Amino-3-(4-hydroxyphenyl)-1-oxopropan-2-ylamino)-1-oxopropan-2-ylamino)-1-oxopropan-2-yl)-1-(5-(hydroxymethyl)thiazol-2-yl)pyrrolidine-2-carboxamide

https://huagongshe.com/reaction/1755474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(S)-N-((S)-1-((S)-1-((S)-1-Amino-3-(4-hydroxyphenyl)-1-oxopropan-2-ylamino)-1-oxopropan-2-ylamino)-1-oxopropan-2-yl)-1-(5-formylthiazol-2-yl)pyrrolidine-2-carboxamideHCID 86700119—
SolventWater ethanolHCID 19096565—
Product(S)-N-((S)-1-((S)-1-((S)-1-Amino-3-(4-hydroxyphenyl)-1-oxopropan-2-ylamino)-1-oxopropan-2-ylamino)-1-oxopropan-2-yl)-1-(5-(hydroxymethyl)thiazol-2-yl)pyrrolidine-2-carboxamideHCID 86700118—

Reaction Steps

Following the procedure as described in Example 32, except using material from Example 81 (6.4 mg, 0.012 mmol), EtOH/H2O (4:1) (3 mL), sodium borohydride (4.2 mg, 0.111 mmol) and stirring at room temp for 2 h, the title compound is isolated (quantitative yield) that is used crude in the next step. LC/MS (Condition A): ret, T=1.54 min, (2M+Na) 1087.51.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169295B2
Source datasetuspto-grants-2015_10
ORD IDord-f9462bcaa6cc418e8adca359040e54e4
Source noteuspto-grants-2015_10