Methanesulfonyl chloride → HCID 58748264, compound

HRID 1162642Notes

Reaction equation

[C:1]([O:5][C:6]([N:8]1[CH2:12][CH:11]([NH:13][C:14]([C:16]2[S:17][C:18]([Cl:21])=[CH:19][CH:20]=2)=[O:15])[C@@H:10]([NH2:22])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:23][S:24](Cl)(=[O:26])=[O:25]>>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH:10]([NH:22][S:24]([CH3:23])(=[O:26])=[O:25])[C@@H:11]([NH:13][C:14]([C:16]2[S:17][C:18]([Cl:21])=[CH:19][CH:20]=2)=[O:15])[CH2:12]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

Reactant 2

HCID 31297Methanesulfonyl chloride

HCID 68646427HCID 68646427, compound

Product 1

HCID 58748264HCID 58748264, compound

Procedure

35.3 In analogy to example 20.2 (S)-3-amino-4-[(5-chloro-thiophene-2-carbonyl)-amino]-pyrrolidine-1-carboxylic acid tert-butyl ester was reacted with methane sulfonylchloride to give (S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-4-methanesulfonylamino-pyrrolidine-1-carboxylic acid tert-butyl ester. White solid. MS 424.0 ([M+H]+)

Sources & evidence

ORD record: ord-28b434c8065e4b00a1d5ac67748caefb
Source dataset: uspto-grants-2010_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07820699B2

Reaction notes

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