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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121200Generated: November 2, 2026

methyl (2S)-2-amino-4-(methylsulfanyl)butanoate → HCID 54128509, compound

https://huagongshe.com/reaction/2121200

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl (2S)-2-amino-4-(methylsulfanyl)butanoateHCID 64684—
ReactantHCID 10570985HCID 10570985—
ProductHCID 54128509HCID 54128509—

Reaction Steps

The desired compound was prepared from 4-(3-pyridylsulfonylmethyl)-2-phenylbenzoic acid methyl ester by saponification of the methyl ester using the procedure of Example 228D, and coupling with methionine methyl ester according to the procedure of Example 186C. mp 152-154° C. 1H NMR (300 MHz, CDCl3) δ 8.95 (d, 1H), 8.87 (dd, 1H), 7.94 (ddd, 1H), 7.66 (d, 1H), 7.43 (m, 4H), 7.30 (m, 2H), 7.21 (dd, 1H), 7.10 (d, 1H), 5.91 (bd, 1H), 4.66 (ddd, 1H), 4.42 (s, 2H), 3.68 (s, 3H), 2.08 (t, 2H), 2.02 (s, 3H), 1.93 (m, 1H), 1.75 (m, 1H). MS (CI NH3) m/e 516 (M+NH4)+, 499 (M+H)+. Anal calc' for C25H26N2O5S2: C, 60.22; H, 5.25; N, 5.62. Found: C, 60.28; H, 4.94; N, 5.56.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693123B2
Source datasetuspto-grants-2004_02
ORD IDord-9a8aeffce0f448e882e85387ac9a707f
Source noteuspto-grants-2004_02